Qa Specialist, Medical Devices (Iso 13485/Mdr)
pEssilorLuxottica in Italy is seeking a QA Specialist to join the Quality Regulatory Affairs team and support the maintenance and continuous improvement of the Quality Management System, ensuring compliance with medical device requirements across the product lifecycle.
/ppYou will collaborate with Production, RD, Regulatory Affairs and suppliers in a dynamic cross?functional environment, drafting procedures, managing CAPAs, audits, and changes to sustain quality throughout the organization.
/p #J-*****-Ljbffr
/ppYou will collaborate with Production, RD, Regulatory Affairs and suppliers in a dynamic cross?functional environment, drafting procedures, managing CAPAs, audits, and changes to sustain quality throughout the organization.
/p #J-*****-Ljbffr